Busch Lab

ZMP

si:rp71-84d19.3

Ensembl ID:
ENSDARG00000075033
ZFIN ID:
ZDB-GENE-070912-719
Description:
GTP-binding protein 8 [Source:UniProtKB/Swiss-Prot;Acc:B0S8I0]
Human Orthologue:
GTPBP8
Human Description:
GTP-binding protein 8 (putative) [Source:HGNC Symbol;Acc:25007]
Mouse Orthologue:
Gtpbp8
Mouse Description:
GTP-binding protein 8 (putative) Gene [Source:MGI Symbol;Acc:MGI:1913317]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa41429 Nonsense Mutation detected in F1 DNA Not yet available
sa5820 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa41429
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111039 Nonsense 217 286 4 6
Genomic Location (Zv9):
Chromosome 9 (position 28366954)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 27522650
GRCz11 9 27333396
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACTGATTTAGTTGCTGTGGAGATGTTTGAAGAATTTAATTTGCCTTA[T/A]GTGGTGAGTGTTTGGCTGAATTTAAATGTGTTTATATAAATAAATAAATA
Long Flanking Sequence:
CTTCTCTCATCCGTGCCTTATTCTCTCTTGCACCAGAGGTGGAAGTGCGGGTCTCTAAAACTCCAGTGAGTATGTATGTCAGGGATGTTCTAGCAATTTATTCCTCTGTAAAATAAAAGTCTAATCTCAACCTAATTCTATATTTTTACACAGGGTCACACCAAAAAGCTCAATTTCTTTACTGTGGGAAAAGCGTTTACTCTAGTAGACATGCCTGGCTATGGACACATGGCACCACAGGACTTTGTAGAGATGGTTGAACCGTATCTTCAGGAGCGCCACAAGTAGGTTGAAGTTACTGCTGTACTTTAACTAATTCCTTATATACTGAAGCTTTATGTGTTTGTGTCTGAATAAATGCATAGTAAAGGGAGTGTTTCGTGATCTCTCATTTTTATCTGTAGTTTGGCGAGGACGTTCTTGCTGGTGGATGCAAGTGCAGGATTGCAGAGTACTGATTTAGTTGCTGTGGAGATGTTTGAAGAATTTAATTTGCCTTA[T/A]GTGGTGAGTGTTTGGCTGAATTTAAATGTGTTTATATAAATAAATAAATATATTATTATTATTATTATTTTGCTCACCTATCACAGTAAGCACAAATATCAAAATGAGGACATTCTGAACTACTTCTATAAGCATTTTTCAAATCAGATACATAGACAATATTTCTACTTTTGTCCTGTTAGTACTCGGGTACATTTGATTTCCTTTAGACTTTCAAGCTACCACAATGCAATGTGGCATATTATCTCACTAAGACAACATTTGAAACAAATATGTCTGTGTACTATATGTGGTAGCACAAAAACAAATTAGAGCTATTGCATACAGGGAGTTTTTTTAGCTACCCAATGATCTGCTGAATTAAAAAAAAACGTTGCTACTGAAAGCTATTTTTATCTACAAGGTGCAGATGTTGCTTTTTTGTAGTAATTAAACACACATATTTGTTTTTTGACAATTCTGCAAATGTTAGCTTCTAAATCTGTATGTCCCGTAGCGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5820
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111039 Nonsense 286 286 6 6
Genomic Location (Zv9):
Chromosome 9 (position 28370237)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 27525933
GRCz11 9 27336679
KASP Assay ID:
554-3515.1 (used for ordering genotyping assays)
KASP Sequence:
ATGTTTCATAGCACACGTAACTGGGAAACAACWGCTTTCTGCTAAACAAT[C/A]ATGAATGTACAGGACTGCCATGCACTGACACCACGTGGACAAATCTCATT
Long Flanking Sequence:
TTACTTTACAAGTGTCATCTTGTTTAAACGTGTTAGAGCAATGATAAGTGTATATTGCGCACTCATCGTTAACCACTTCTTTAGGTTTTATGTGAGTATGAGTGTACATTTGAGGTACCCTTGAACGCAGCAATTCCATAAATCCTGTGTACAAATATTTCACAGCATCTGACCCATAGTTTTATAAGCATGGTGAACATTCTGTGTTAGGAGAAATATGTTAATGTGGTCTGATTATTATCAACTGATAACAGTAAGCTGATAAGATAAGGCTAGTGGTTCTGGAAACAGTTGCAGTTTATTTTCGTGTCAATACAGTAAGTCATTTTCTCACAGATAAGGTGATAAGTAACATGGGTTATTACATTCTTACACCTAATTTTATTTCTCTCTTCCGTTCCTTTCTATAACCCGCAGTTCAGTCCAATTCTCCGGGATTCACCTGCTCAGATGTTTCATAGCACACGTAACTGGGAAACAACTGCTTTCTGCTAAACAAT[C/A]ATGAATGTACAGGACTGCCATGCACTGACACCACGTGGACAAATCTCATTTCCAAAACACATTTTGAAAAAGACCAATTTTAAGCATAGAAATGTTGATGTCGAGTCTGTGCATTAATGACTAATGCAGAGGAATCATGTTGTTACTGGTTTCAGGATTCATTCAACCCTGTATGAACTCCATGAATGATCCAGGATTGAGTGTGAGTGAGCTTTCAGAGGAAATAAGAAAAATTTTAATTTTTGTAAATGGTATCATGGCATAGTACATACACACTGATATTAGTCGCAGTGATTAAAAAAATGAAGAAATTTACCATGTGGAATTAACTCCATGCTTCATATACAGATTGTATAAATTCAACCTAAAAGTTACTGTTGAAACCTGTATTTGCTGTAGAATAATTTTCATAATCGTTCAAAATCATTTATTTTTGTGCATTTCATCGATCTATTTCATTTAGTCTATGACATTTCAGTCAAATCAATTAAATACTATGA
Associated Phenotype:
Not determined